REACTIONS OF 1,5-DIKETONES WITH AMMONIA AND ITS DERIVATIVES

Authors

  • В. Г. Харченко N. G. Chernyshevskii Saratov State University, Saratov
  • Л. И. Маркова N. G. Chernyshevskii Saratov State University, Saratov
  • О. В. Федотова N. G. Chernyshevskii Saratov State University, Saratov
  • Н. В. Пчелинцева N. G. Chernyshevskii Saratov State University, Saratov

Keywords:

alkylidenedicyclanones, arylidenedicyclanones, aroylpyrroles, 3-hydroquinol-2-ones, dihydro-1,2-diazepines, N-R-dihydropyridines, dihydropyridines, tetrahydropyridines, 1,5-diketones, octahydroacridines, pentane-1,5-diones, 2-pentene-1,5-diones, pyrazolines, pyrazoles, pyridines, pyridine bases, piperidine bases, semicyclic, oxosemicyclic 1,5-diketones, pyridinium salts, tetrahydroquinolines, azaheterocyclization, indolization, pyridinization, properties, synthesis, structure

Abstract

Published data and the authors' own experimental results on the reaction of aliphatic, semicyclic, and oxosemicyclic 1,5-diketones and alkylidene- and arylidene-2,2-dicyclanones with ammonia, ammonium acetate, and XNH2 derivatives, where X = Alk, Ar, OH, NH2, PhNH, ArCONH, and CHO, are reviewed. The characteristics and the relationships governing the transformations into azaheterocycles in relation to the nature of the reagents and the reaction conditions are discussed.

How to Cite
Kharchenko, V. G.; Markova, L. I.; Fedotova, O. V.; Pchelintseva, N. V. Chem. Heterocycl. Compd. 2003, 39, 1121. [Khim. Geterotsikl. Soedin. 2003, 1283.]

For this article in the English edition, see DOI 10.1023/B:COHC.0000008257.42400.9e

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Published

2003-09-25

Issue

No. 9 (2003)

Section

Review Articles